nsv3071841
- Organism: Homo sapiens
- Study:nstd90 (dbSNP curated variants)
- Variant Type:insertion
- Method Type:Curated
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
- Data Source:HUMANGENOME_JCVI
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 95 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 95 SVs from 22 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv3071841 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 76,232,006 | 76,232,006 |
| nsv3071841 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 76,698,349 | 76,698,349 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv14042852 | insertion | 1104685289991 | Curated | Curated |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv14042852 | Remapped | Perfect | NC_000014.9:g.7623 2006_76232007ins23 1 | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 76,232,006 | 76,232,006 |
| nssv14042852 | Submitted genomic | NC_000014.8:g.7669 8349_76698350ins23 1 | GRCh37 (hg19) | NC_000014.8 | Chr14 | 76,698,349 | 76,698,349 |